This invention discloses a
temperature gradient cell capture culture
chip device and method, comprising a
cell capture culture
chip, a temperature conduction film, and a
temperature gradient chip. The
cell capture culture chip is provided with an inlet, an
inlet channel, an outlet channel, and an outlet, with the inlet and outlet channels correspondingly connected to cell capture culture chambers. The
temperature gradient chip is provided with several heating channels, the interior of which is filled with
liquid metal material. Each heating channel includes several semi-annular cavities and several linear cavities. The semi-annular cavities on the heating channels combine to form a circular heating area. This invention enables on-chip
cell culture studies under dual-factor stimulation conditions of
drug concentration gradient and temperature gradient, supporting efficient localization and long-term stable culture of target cells. It can also synergistically apply dual-factor stimulation conditions of
drug concentration gradient and temperature gradient, allowing real-time observation of cell proliferation behavior under these stimulation conditions and subsequent
metabolite and genomic analysis.